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Items: 1 to 20 of 90

1.

The high spontaneous mutation rate: is it a health risk?

Crow JF.

Proc Natl Acad Sci U S A. 1997 Aug 5;94(16):8380-6. Review.

2.

How much do we know about spontaneous human mutation rates?

Crow JF.

Environ Mol Mutagen. 1993;21(2):122-9. Erratum in: Environ Mol Mutagen 1993;21(4):389.

PMID:
8444142
3.

Spontaneous mutation as a risk factor.

Crow JF.

Exp Clin Immunogenet. 1995;12(3):121-8. Review.

PMID:
8534499
4.

The origins, patterns and implications of human spontaneous mutation.

Crow JF.

Nat Rev Genet. 2000 Oct;1(1):40-7. Review.

PMID:
11262873
5.

Alport syndrome. Molecular genetic aspects.

Hertz JM.

Dan Med Bull. 2009 Aug;56(3):105-52.

PMID:
19728970
6.
7.

The observed human sperm mutation frequency cannot explain the achondroplasia paternal age effect.

Tiemann-Boege I, Navidi W, Grewal R, Cohn D, Eskenazi B, Wyrobek AJ, Arnheim N.

Proc Natl Acad Sci U S A. 2002 Nov 12;99(23):14952-7. Epub 2002 Oct 23.

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13.

[Mutagenic effect of advanced paternal age in neurocardiofaciocutaneous syndrome].

Seemanov√° E, Zenker M.

Cas Lek Cesk. 2014;153(5):242-5. Czech.

PMID:
25370770
14.

Direct estimation of the mitochondrial DNA mutation rate in Drosophila melanogaster.

Haag-Liautard C, Coffey N, Houle D, Lynch M, Charlesworth B, Keightley PD.

PLoS Biol. 2008 Aug 19;6(8):e204. doi: 10.1371/journal.pbio.0060204.

15.
16.

Germ-line origins of mutation in families with hemophilia B: the sex ratio varies with the type of mutation.

Ketterling RP, Vielhaber E, Bottema CD, Schaid DJ, Cohen MP, Sexauer CL, Sommer SS.

Am J Hum Genet. 1993 Jan;52(1):152-66.

17.

Mutations causing hemophilia B: direct estimate of the underlying rates of spontaneous germ-line transitions, transversions, and deletions in a human gene.

Koeberl DD, Bottema CD, Ketterling RP, Bridge PJ, Lillicrap DP, Sommer SS.

Am J Hum Genet. 1990 Aug;47(2):202-17.

18.

The fitness effects of spontaneous mutations in Caenorhabditis elegans.

Vassilieva LL, Hook AM, Lynch M.

Evolution. 2000 Aug;54(4):1234-46.

PMID:
11005291
20.

Genome wide spontaneous mutation in human cells determined by the spectrum of mutations in hprt cDNA genes.

Lichtenauer-Kaligis EG, Thijssen J, den Dulk H, van de Putte P, Tasseron-de Jong JG, Giphart-Gassler M.

Mutagenesis. 1993 May;8(3):207-20.

PMID:
8332083

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